scholarly journals The role of metal–support interaction for CO-free hydrogen from low temperature ethanol steam reforming on Rh–Fe catalysts

2017 ◽  
Vol 19 (6) ◽  
pp. 4199-4207 ◽  
Author(s):  
Catherine K. S. Choong ◽  
Luwei Chen ◽  
Yonghua Du ◽  
Martin Schreyer ◽  
S. W. Daniel Ong ◽  
...  
Keyword(s):  
Steam Reforming ◽  
Active Sites ◽  
Support Interaction ◽  
Metal Support Interaction ◽  
Free Hydrogen ◽  
Metal Support ◽  
Fe Catalysts ◽  
Ethanol Steam

Effect of metal–support interaction on the generation of Rh–FexOy active sites is investigated via various in situ techniques.

Zirconia-Supported Monometallic Ru and Bimetallic Ru-Sn, Ru-Fe Catalysts: Role of Metal Support Interaction in the Hydrogenation of Cinnamaldehyde

1994 ◽  
Vol 98 (40) ◽  
pp. 10180-10188 ◽  
Author(s):  
Bernard Coq ◽  
Pramod S. Kumbhar ◽  
Claude Moreau ◽  
Patrice Moreau ◽  
Francois Figueras
Keyword(s):  
Support Interaction ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Fe Catalysts

Co-processing of hydrodeoxygenation and hydrodesulfurization of phenol and dibenzothiophene with NiMo/Al2O3–ZrO2 and NiMo/TiO2–ZrO2 catalysts

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Jesús Andrés Tavizón Pozos ◽  
Gerardo Chávez Esquivel ◽  
Ignacio Cervantes Arista ◽  
José Antonio de los Reyes Heredia ◽  
Víctor Alejandro Suárez Toriello
Keyword(s):  
Active Sites ◽  
Reaction Rate ◽  
Supported Catalysts ◽  
Initial Reaction Rate ◽  
Initial Reaction ◽  
Competition Effect ◽  
Support Interaction ◽  
Highly Active ◽  
Metal Support Interaction ◽  
Metal Support

Abstract The influence of Al2O3–ZrO2 and TiO2–ZrO2 supports on NiMo-supported catalysts at a different sulfur concentration in a model hydrodeoxygenation (HDO)-hydrodesulfurization (HDS) co-processing reaction has been studied in this work. A competition effect between phenol and dibenzothiophene (DBT) for active sites was evidenced. The competence for the active sites between phenol and DBT was measured by comparison of the initial reaction rate and selectivity at two sulfur concentrations (200 and 500 ppm S). NiMo/TiO2–ZrO2 was almost four-fold more active in phenol HDO co-processed with DBT than NiMo/Al2O3–ZrO2 catalyst. Consequently, more labile active sites are present on NiMo/TiO2–ZrO2 than in NiMo/Al2O3–ZrO2 confirmed by the decrease in co-processing competition for the active sites between phenol and DBT. DBT molecules react at hydrogenolysis sites (edge and rim) preferentially so that phenol reacts at hydrogenation sites (edge and edge). However, the hydrogenated capacity would be lost when the sulfur content was increased. In general, both catalysts showed similar functionalities but different degrees of competition according to the highly active NiMoS phase availability. TiO2–ZrO2 as the support provided weaker metal-support interaction than Al2O3–ZrO2, generating a larger fraction of easily reducible octahedrally coordinated Mo- and Ni-oxide species, causing that NiMo/TiO2–ZrO2 generated precursors of MoS2 crystallites with a longer length and stacking but with a higher degree of Ni-promotion than NiMo/Al2O3–ZrO2 catalyst.

Strong metal-support interaction in Ni/TiO2 catalysts: in situ EXAFS and related studies

1993 ◽  
Vol 17 (1-2) ◽  
pp. 29-37 ◽  
Author(s):  
T. Arunarkavalli ◽  
G. U. Kulkarni ◽  
G. Sankar ◽  
C. N. R. Rao
Keyword(s):  
Support Interaction ◽  
Metal Support Interaction ◽  
Metal Support ◽  
In Situ Exafs ◽  
Strong Metal Support Interaction

Enhancing metal–support interaction by in situ ion-exchanging strategy for high performance Pt catalysts in hydrogen evolution reaction

2020 ◽  
Vol 8 (32) ◽  
pp. 16582-16589 ◽  
Author(s):  
Xulei Sui ◽  
Lei Zhang ◽  
Junjie Li ◽  
Kieran Doyle-Davis ◽  
Ruying Li ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
High Performance ◽  
Pt Catalysts ◽  
Acidic Media ◽  
Support Interaction ◽  
Metal Support Interaction ◽  
Metal Support ◽  
Metal Support Interactions

A facile in situ ion-exchanging strategy directly enhances metal–support interactions between Pt and support and promotes HER electrocatalytic performance in acidic media.

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